rs34281605

Homo sapiens
G>A
C15orf53 : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
A=0244 (7304/29868,GnomAD)
A=0249 (7274/29118,TOPMED)
A=0178 (891/5008,1000G)
A=0311 (1198/3854,ALSPAC)
A=0314 (1164/3708,TWINSUK)
chr15:38697473 (GRCh38.p7) (15q14)
AD
GWASdb2
1   publication(s)
See rs on genome
8 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 15NC_000015.10:g.38697473G>A
GRCh37.p13 chr 15NC_000015.9:g.38989674G>A

Gene: C15orf53, chromosome 15 open reading frame 53(plus strand)

Molecule type Change Amino acid[Codon] SO Term
C15orf53 transcriptNM_207444.2:c.N/AIntron Variant

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.826A=0.174
1000GenomesAmericanSub694G=0.750A=0.250
1000GenomesEast AsianSub1008G=0.968A=0.032
1000GenomesEuropeSub1006G=0.740A=0.260
1000GenomesGlobalStudy-wide5008G=0.822A=0.178
1000GenomesSouth AsianSub978G=0.800A=0.200
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.689A=0.311
The Genome Aggregation DatabaseAfricanSub8680G=0.806A=0.194
The Genome Aggregation DatabaseAmericanSub836G=0.750A=0.250
The Genome Aggregation DatabaseEast AsianSub1620G=0.972A=0.028
The Genome Aggregation DatabaseEuropeSub18430G=0.713A=0.286
The Genome Aggregation DatabaseGlobalStudy-wide29868G=0.755A=0.244
The Genome Aggregation DatabaseOtherSub302G=0.730A=0.270
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.750A=0.249
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.686A=0.314
PMID Title Author Journal
23089632A genome-wide association study of alcohol-dependence symptom counts in extended pedigrees identifies C15orf53.Wang JCMol Psychiatry

P-Value

SNP ID p-value Traits Study
rs342816051.25E-07alcohol dependence23089632

eQTL of rs34281605 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
There is no eQTL annotation for this SNP

meQTL of rs34281605 in Fetal Brain

Probe ID Position Gene beta p-value
cg21039679chr15:38989738C15orf53-0.02718181485713934.9448e-16

Genomic View

Chromatin Interaction

There is no significant Hi-C chromatin interaction data for this SNP.

Enhancer Annotation (GRCh37.p13)

Chromosome Start End Region Distance ( -/+ : Up/Downstream )
chr153896065238961725E068-27949
chr153896065238961725E069-27949
chr153896065238961725E070-27949
chr153894079638940926E071-48748
chr153900002839001434E08110354
chr153900646639007349E08116792
chr153896051838960573E082-29101
chr153896065238961725E082-27949